Tag | Content |
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EnhancerAtlas ID | HS175-25784 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr6:30483530-30484960 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr6:30484034-30484046 | AGGTAAACAGAA | + | 6.14 | POU4F2 | MA0683.1 | chr6:30484255-30484271 | GAGAATATTTAATGAA | + | 6.09 | TEAD1 | MA0090.2 | chr6:30484184-30484194 | CACATTCCAT | + | 6.02 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_20955 | chr6:30483089-30484988 | CD8_Memory_7pool | SE_51043 | chr6:30482661-30484841 | Sigmoid_Colon | SE_53014 | chr6:30482775-30484845 | Small_Intestine | SE_53611 | chr6:30482485-30485328 | Spleen | SE_62602 | chr6:30456364-30512797 | Tonsil | SE_65627 | chr6:30483105-30485215 | Pancreatic_islets |
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Enhancer Sequence | TTGAGACGGA GTTTCGCTCT TGCCGCTGCC CAGGCTATAG TGCAATGGCG CCATCTCGGC 60 TCACCGCAAC TTCCGCCTCC CAGGTTCAAG CGATTCTCCT GCCTCAGCCT CCCGAGTAGC 120 TTGTATTACA GGCATGCGCC ACCACACCCG GCTAATTTTG TATTTTTAGT AGAGAGGGGG 180 TTTCTCCATG TTGTTCAGGC TGGTCTCGAA CTCCCAACCT CAGGTGATCC GCCTGTCTTG 240 GCCTCTCAAG TGCTGGGATT ACAGGGGTGA GCCACCGCGC CCAGCCGGGA GCCCCTATTT 300 TAAGGACGCT ATTGCTGTGG AGGAGTAACC CCACTTTTAG GAATCCTTTT CCGTGCGAAA 360 GGCTGTTTGA GATCAGGCGC AACAACTTCT CCCGCTCAGG TTACCCTCAG AAAGGCTATG 420 GACCCCGGAC TCCGCCCCAG ATTGCATAAC AACTGAGGGG TGGGTCCCTA TTTCCTCTCT 480 GGGATCTGTA GCCAATCATT CACGAGGTAA ACAGAACGAC CGAGTTTCTC TCAGCCGAGA 540 ACTGTGGCTG CCCCTCCGGT GAAAACAGAG GAAGTGGGAG CGGCAGGAAG CGCTTTGGGA 600 CCAGGGCGAC CCCTGAAGCG TAGAGGAACC AGGTCACAAG CATACGTGAA TGCTCACATT 660 CCATAGTTAT CAAATGTATT CAGGTTTAAA TTTTACTTTT CTAGAAAAAA TGTAAATAAT 720 CCGTTGAGAA TATTTAATGA AAAATGTTGG TCGTATCTTT ATCTGGTCTG CGGCTCTGTC 780 CCTGTTTCCT GGATAGGAGA CTACGTCTGT ATCTTGTATC ACAGGAGGCA CCTTCTTCCT 840 GTTTCCTGGC ACAGACTTGT AAGTGAATTT CCTGCCCGCC TCCGCCCACA GCGTAAGCCG 900 CGCTGGAACA GCTCACTTAT TGCCCCAGAT GTATGTGGAG TAACCGCCTT CAGTTTCCTG 960 GTTCTGAGTT TCCGTGTTAC TCAAGCAATG CTTCTGCTGA ATTTGTCTTT TTTTTTTTTT 1020 TGAGACAGAG TCTTGCTTTG TCGCCCAGAC TGGAGTGAAA TGGCGTGGTC TCGGCTCACT 1080 GCAGCCTCCA CCTCCTGGGT TCAAGCGAGT CTCCTGCCTC AGCCTCCTGA GTGTGCAACT 1140 TATCTTTTTA TTTTATTTAT TTATAATTTT TTGGCTAATT TTGGCTATTT TGTGTCTGTG 1200 TGTGTATTTT TAGTAGACAT GGGGTTTCAC CATGTTGGGC AGGCTGGTCT CGAACTCCTG 1260 ACCTCAGGTG ATCCGCCCAC CTCGGCCTCC CAAAGTGCTG GAATTACAGG CGTGAGCCAC 1320 CGCACCTGGC CTATTTATTT ATTTATTTAT TTGTGACTGA GTCTCGCTCT GTCACCCAAG 1380 CTGGAATGCA ATGGCGTGAT CTCGGCTCAC TGCTACCTCC ACGCCCCAAG 1430
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